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KGA-2727

    
98%

KGA-2727

源叶(MedMol)
S55502 一键复制产品信息
666842-36-0
C26H40N4O8
536.62
Propanamide,3-​[[3-​[4-​[[3-​(β-​D-​glucopyranosyloxy)​-​5-​(1-​methylethyl)​-​1H-​pyrazol-​4-​yl]​methyl]​-​3-​methylphenoxy]​propyl]​amino]​-
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S55502-1mg促销
98%

¥756.00 ¥680.00

货期:3-5天 - - - -
S55502-5mg促销
98%

¥2640.00 ¥2370.00

7 - - - -
S55502-10mg促销
98%

¥4350.00 ¥3910.00

5 - - - -
S55502-25mg促销
98%

¥7630.00 ¥6860.00

3 - - - -
S55502-50mg促销
98%

¥12100.00 ¥10900.00

2 - - - -
S55502-100mg促销
98%

¥15200.00 ¥13700.00

3 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
靶点: Ki: 97.4 nM (human SGLT1), 43.5 nM (rat SGLT1)
体内研究: In the oral glucose tolerance test with streptozotocin-induced diabetic rats, KGA-2727 attenuates the elevation of plasma glucose after glucose loading, indicating that KGA-2727 improves postprandial hyperglycemia.
In Zucker diabetic fatty (ZDF) rats, chronic treatments with KGA-2727 reduces the levels of plasma glucose and glycated hemoglobin. Furthermore, KGA-2727 preserves glucose-stimulated insulin secretion and reduces urinary glucose excretion with improved morphological changes of pancreatic islets and renal distal tubules in ZDF rats.
参考文献: 1. Shibazaki T, et al. KGA-2727, a novel selective inhibitor of a high-affinity sodium glucose cotransporter (SGLT1), exhibits antidiabetic efficacy in rodent models. J Pharmacol Exp Ther. 2012 Aug;342(2):288-96.
保存条件: -20°C
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.864 ml 9.318 ml 18.635 ml
5 mM 0.373 ml 1.864 ml 3.727 ml
10 mM 0.186 ml 0.932 ml 1.864 ml
50 mM 0.037 ml 0.186 ml 0.373 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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